- 更多网络例句与环生成元相关的网络例句 [注：此内容来源于网络，仅供参考]
-
In addition, the carbon chain of butylene glycol was longer than that of ethylene glycol, so the spatial hindrance of butylene glycol was bigger than that of ethylene glycol, so the reaction rate of butylene glycol was longer than that of ethylene glycol.
由邻位化合物生成的五元环络合物比由间位化合物形成的六元环络合物稳定性高，反应速度快。
-
In this paper, after the introduction of the basic concepts and the main results on K〓 theory, relative K〓 theory and the theory of classical groups of degree 2 which is related to K〓 theory, we study the problems of the computation of K〓 for the ring of integers of quadratic imaginary fields, examples of subrings of quadratic fields which are not universal for GE〓 and generating set of the Cokernel of the canonical homomorphism from K〓 to K〓.
本文在介绍了K〓理论和相对K〓理论以及与K〓理论有关的2阶典型群的基本概念及主要成果之后，对于虚二次域代数整环的K〓群的计算，非GE〓泛的虚二次域的子环以及K〓到K〓的自然同态的余核的生成元集等问题进行了研究。
-
For distinctly understanding the mutual influence between the structural units, a series of compounds from five and six-membered C-N heterocycle substituting the tetrazine ring are designed. These several types of compounds are studied by means of the quantum chemistry calcualtions and discussed the influence of the structural units upon the main performance (heat of formation, density, velocity and pressure of detonation) and found out the best combination of performance.
为了更清楚的了解结构单元之间的相互影响，设计了六元氮杂环和五元氮杂环取代1，2，4，5-四嗪得到了一系列化合物，采用量子化学计算方法对它们进行了详细的理论研究，讨论了各种氮杂环的改变对四嗪类化合物性能(包括生成热、密度以及爆速和爆压等)的影响，并找出爆轰性能较好的结构单元组合。
-
In this paper,we determine J_~(2~k+2v)by constructing ingeniously indecomposable manifolds M,which can be generators in MO_*,and defining appropriate(Z_2)~k-action on M.
在本文中，我们通过巧妙地构造流形M，使其所在的上协边类不可分解，从而可以作为上协边环MO_*的生成元，并在M上定义适当的(Z_2)~k作用使其不动点集F具有常余维数r，决定了未定向上协边环MO_*的理想J_~(2~k+2v)。
-
Using the presentation, suppose that M is the maximal ideal of a commutative local domain R and R/M=F〓 is a finite field with q elements, a generating set of elements at most is obtained for K=Coker K〓
设M为交换局部整环R中极大理想，R/M〓F〓为q元有限域，由这个表现得到了K=Coker的一个至多含有个元素的生成元集。
-
In order to obtained the six-membered ring compound and a thorough assignment of the spectra, and further to prove that the six-membered ring compound was formed from the hydrogen transfer, the compound N-butyl-4-(N-methylphenylamino)-5-amino- 1, 8-naphthalimide 6 was designed to obtained with N-butyl-4-bromo-5-amino-1, 8-naphthalimide and N-methyl phenylamine as the starting material. However it was difficult to obtain the desired product as the different solvent giving the different products except the desired product.
为了能够得到六元环化合物作为定标的物质及其确切的谱图分析结果，并且为了进一步证明由五元环产物通过氢转移得到六元环产物的正确性，设计用N-丁基4-溴-5-氨基-1，8-萘酰亚胺与N-甲基苯胺反应生成N-丁基-4--5-氨基-1，8-萘酰亚胺6，结果发现这种方法很难实现，选择不同的溶剂会生成不同的产物，却都不是目标产物。
-
The results showed that hydrogen peroxide, silanols species and TiO〓 didn't have solvolysis activity of propylene oxide. While framework Al, coordinatively unsaturated Ti〓 ions as Lewis acid sites in the framework, Ti-OH and the five member ring active titanium species formed by TS-1, hydrogen peroxide and solvent can catalyze the solvolysis of propylene oxide.
研究结果表明：原料双氧水和TS-1沸石上的SiOH和TiO〓对环氧丙烷溶剂解反应无催化活性；而下列物种对环氧丙烷溶剂解反应具有催化活性：TS-1中的骨架铝，沸石骨架中配位不饱和的Ti〓形成的L酸中心，TS-1水解产生的钛羟基和由TS-1，双氧水和溶剂相互作用所生成的五元环中间活性钛物种。
-
Pastijn left the question open whether is a congruence on the free idempotent semiring generated by two free generators. In this paper, the open question will be solved.
从而，提出了一个公开问题：是否为由两个自由生成元生成的幂等元半环上的同余，本文给出了这个问题的一个肯定的回答。
-
Due to the ring strain and Lewis acid character, silacyclobutanes and silacyclobutenes can undergo ring expansion reactions to afford five- and six-membered silacycles, or ring opening to give organosilicon molecules and materials as well as fulfill organic transformations under very mild conditions.
硅杂环丁烷和硅杂环丁烯由于存在环张力和具有一定的Lewis酸性，能够通过扩环反应生成五元和六元含硅杂环化合物，也能够通过开环反应生成不同结构的有机硅分子和聚合物，抑或实现有机反应在温和条件下的转化。
-
From the potential energy profile, it can be predicted that, the dominant channel of this reaction consists of three steps: the two reactants first form a three-membered ring intermediate (INT1) through a barrier-free exothermic reaction of 19.2 kJ/mol; three-membered ring intermediate (INT1) isomerizes to a four-membered ring silylene(P2) via the transition state (TS2) with an energy barrier of 22.8 kJ/mol; four-membered ring silylene(P2) further reacts with ethene(R2) to form a silicic bis-heterocyclic compound (P3), which is also a barrier-free exothermic reaction of 132.2 kJ/mol.
用CCSD//MP2/6-31G*方法研究了单重态二甲基亚烷基硅烯与乙烯生成硅杂双环化合物环加成反应的机理，根据该反应的势能面可以预言，该反应的主反应通道有三步组成：第一步是两反应物（R1， R2）首先生成了一三元环中间体（INT1），它是一无势垒的放热反应，放出的能量为19.2 kJ/mol；第二步是三元环中间体(INT1)经过渡态TS2异构化为了四元环硅烯（P2），其势垒为22.8 kJ/mol；第三步是四元环硅烯（P2）进一步与乙烯(R2)反应生成了硅杂双环化合物（P3），该反应也是一无势垒的放热反应，放出的能量为132.2 kJ/mol。
- 更多网络解释与环生成元相关的网络解释 [注：此内容来源于网络，仅供参考]
-
ring extension：环扩张
ring axioms 环公理 | ring extension 环扩张 | ring generator 环生成元
-
ring generator：环生成元
ring extension 环扩张 | ring generator 环生成元 | ring homomorphism 环同态
-
ring homomorphism：环同态
ring generator 环生成元 | ring homomorphism 环同态 | ring of endomorphisms 自同态环